NCT05191992

Brief Summary

The experimentally planned research was carried out between the dates of 01.06.2021-10.11.2021 with the students of ……………. Faculty of Health Sciences, Department of Nursing. The students, whose informed consent form was obtained beforehand, were provided to fill in the Participant Diagnosis Form and the Basic Life Support Information Evaluation Form questioning their demographic characteristics before the education. Afterward, with the e-learning method (Perculus 3 Virtual Classroom), the students have given Basic Life Support training in accordance with the AHA 2020 guidelines through a Powerpoint presentation. After the training, the information evaluation form was filled in again by the students in an electronic environment. Afterward, the students were shown how to make a Basic Life Support manikin with a pillow and plastic pet bottle, and the CPR performance was explained with the manikin. The students who made the performance in the home environment made a video recording and uploaded the videos they took to the system within 1 day. Two researchers who are experts in their fields made the video evaluations according to the basic life support performance evaluation form. Later, in the online debriefing session, the pros and cons of the training were discussed with the students, and after 1 month, knowledge and skills were evaluated again and the level of permanence on the subject was measured.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
148

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jun 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2021

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2021

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 10, 2021

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

November 16, 2021

Completed
2 months until next milestone

First Posted

Study publicly available on registry

January 14, 2022

Completed
Last Updated

January 14, 2022

Status Verified

December 1, 2021

Enrollment Period

1 month

First QC Date

November 16, 2021

Last Update Submit

December 29, 2021

Conditions

Keywords

nursing studentcardiopulmonary resuscitationmannequinseducation

Outcome Measures

Primary Outcomes (4)

  • Increasing the effectiveness of BLS training on knowledge given with by e-learning method

    CPR training given with the e-learning method cannot contribute to skill development since there is no mannequin access. The opportunity to practice with the handmade, inexpensive mannequin provided ensures that the training is effective. The effectiveness of the training was evaluated with the 10-question BLS knowledge evaluation form which was organized according to the AHA guideline by authors. In the evaluation of the 10-question knowledge test, each question is 1 point. If the evaluation score is over 70%, it indicates that the participant is successful.

    1 month

  • Increasing the effectiveness of BLS training on skills given with by e-learning method

    CPR training given with the e-learning method cannot contribute to skill development since there is no mannequin access. The opportunity to practice with the handmade, inexpensive mannequin provided ensures that the training is effective. The effectiveness of the training was evaluated with the 20-item BLS Skills Assessment Form, which was organized according to the AHA guideline by authors. In the evaluation of the 20-question BLS Skills Assessment Form, each item is 1 point. If the assessment score is over 70%, it indicates that the participant is successful.

    1 month

  • Increasing the permanence of BLS training on knowledge given by e-learning method

    Studies have reported that the effectiveness of BLS training decreases over time. It is expected that the education method supported by e-learning and handmade mannequins will contribute to the permanence of education by allowing the application to be repeated independently of time, place, and expensive materials. The permanence of the training was evaluated with the 10-question BLS knowledge evaluation form which was organized according to the AHA guideline by authors. In the evaluation of the 10-question knowledge test, each question is 1 point. If the evaluation score is over 70%, it indicates that the participant is successful.

    1 month

  • Increasing the permanence of BLS training on skills given by e-learning method

    Studies have reported that the effectiveness of BLS training decreases over time. It is expected that the education method supported by e-learning and handmade mannequins will contribute to the permanence of education by allowing the application to be repeated independently of time, place, and expensive materials. The permanence of the training was evaluated with the 20-item BLS Skills Assessment Form, which was organized according to the AHA guideline by authors. In the evaluation of the 20-question BLS Skills Assessment Form, each item is 1 point. If the assessment score is over 70%, it indicates that the participant is successful.

    1 month

Study Arms (1)

experimental

EXPERIMENTAL

The group will receive CPR training with the e-learning method and will learn skills with a handmade mannequin.

Other: CPR training with e-learning with a handmade mannequin.

Interventions

The group, who was given theory training with the e learning method, will be taught to make pillows and plastic bottles and cpr mannequins, and they will be asked to practice. Knowledge and skills assessment will be made before, immediately after and 1 month after the training.

experimental

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Volunteering to participate the study,
  • Having taken basic nursing education courses

You may not qualify if:

  • Not wanting to participate in the study,
  • Not taking basic nursing education courses

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zonguldak Bülent Ecevit University

Zonguldak, Merkez, 67100, Turkey (Türkiye)

Location

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD. Research Assistant

Study Record Dates

First Submitted

November 16, 2021

First Posted

January 14, 2022

Study Start

June 1, 2021

Primary Completion

July 1, 2021

Study Completion

November 10, 2021

Last Updated

January 14, 2022

Record last verified: 2021-12

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL
Time Frame
12 months

Locations